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Comparing Two Nerve Block Methods for Pain Relief in Laparoscopic Hernia Surgery

NCT07676123 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2026-06-30

No results posted yet for this study

Summary

After inguinal hernia repair, patients having chronic pain approximately 20 percent. If patients don't have postoperatively acute pain, they will tend to have less chronic pain. The purpose of study is to make people have less pain, even better not to have any. In this study, patients will have preemptive nerve blockage and by this way, they will have less acute and chronic pain.

Conditions

  • MeSH C23.300.707.374.875
  • MeSH E01.370.388.250.520
  • MeSH E03.155.086.711
  • MeSH C23.550.767.700
  • MeSH C23.550.767.859

Interventions

PROCEDURE

Anterior Quadratus Lumborum Block

The procedure will be performed under general anesthesia using 20 ml 0.25% bupivacaine

PROCEDURE

Ilioinguinal-Iliohypogastric Block

The procedure will be performed under general anesthesia using 15 ml of 0.25% bupivacaine.

Sponsors & Collaborators

  • Ankara University

    lead OTHER

Principal Investigators

  • Süheyla Karadağ Erkoç, Assoc. Prof. Dr. · Ankara University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-26
Primary Completion
2026-02-26
Completion
2026-06-26

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07676123 on ClinicalTrials.gov